510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K172862Substantially Equivalent

Portable ECG Monitor (ECG3)

Andon Health Co., Ltd, Tianjin, CN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K172862 is the FDA 510(k) clearance record for Portable ECG Monitor (ECG3), a class II device, cleared for Andon Health Co, Ltd. on under FDA product code DSH (Recorder, Magnetic Tape, Medical). FDA records list 92 510(k) clearances for Andon Health Co, Ltd., from to . As of , FDA records show no recalls naming K172862.

Clearance record

Decision date
Received
(307 days to decision)
Product code
DSH Recorder, Magnetic Tape, Medical
Regulation
21 CFR 870.2800
Device class
Class II
Review panel
Cardiovascular
Applicant
Andon Health Co, Ltd. # 3 Jin Ping St.,Ya An Rd., Tianjin, CN
510(k) summary
Statement
Third party review
No

Clearances, product code DSH

Trailing 12 months
3 clearances under product code DSH in the twelve months to October 2026, December 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code DSH, trailing twelve months
MonthClearances
November 20250
December 20251
January 20260
February 20260
March 20260
April 20261
May 20260
June 20260
July 20261
August 20260
September 20260
October 20260